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伴有颈内静脉错构瘤样改变的先天性纤维脂肪瘤：首例发表病例报告

Congenital Fibrolipoma with Hamartomatous Changes of the Internal Jugular Vein: First Published Case Report.

作者信息

Regal Samer, Khafagy Tamer A, AbdelGawad Mohamed S, Saad Ehab M, Ali Ahmed A

机构信息

Cardiothoracic and Vascular Surgery Center, University Hospital, Mansoura University, Dakahliya, Egypt.

出版信息

Methodist Debakey Cardiovasc J. 2024 Dec 26;20(1):113-118. doi: 10.14797/mdcvj.1519. eCollection 2024.

DOI:10.14797/mdcvj.1519
PMID:39735207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11673465/
Abstract

A 25-year-old female presented with a congenital painless growing mass on the right side of her neck with symptoms of tinnitus and difficulty breathing. Imaging revealed an aneurysm of the internal jugular vein reaching a maximum diameter of 9.2 cm, shifting the trachea and right thyroid lobe to the left side. Simple excision was sufficient to treat compression symptoms and prevent potential thrombosis and embolism. This is the first reported case of aneurysmal internal jugular vein with fibrofatty degeneration and hamartomatous wall morphology associated with compression symptoms.

摘要

一名25岁女性因右侧颈部先天性无痛性生长肿物就诊，伴有耳鸣和呼吸困难症状。影像学检查显示颈内静脉动脉瘤，最大直径达9.2厘米，气管和右侧甲状腺叶向左移位。单纯切除足以治疗压迫症状并预防潜在的血栓形成和栓塞。这是首例报告的伴有纤维脂肪变性和错构瘤样壁形态且伴有压迫症状的颈内静脉动脉瘤病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/f43b21ca4fb4/mdcvj-20-1-1519-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/d43cc598e326/mdcvj-20-1-1519-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/d37cdeea47da/mdcvj-20-1-1519-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/f43b21ca4fb4/mdcvj-20-1-1519-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/d43cc598e326/mdcvj-20-1-1519-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/d37cdeea47da/mdcvj-20-1-1519-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2901/11673465/f43b21ca4fb4/mdcvj-20-1-1519-g3.jpg

相似文献

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Congenital Fibrolipoma with Hamartomatous Changes of the Internal Jugular Vein: First Published Case Report.伴有颈内静脉错构瘤样改变的先天性纤维脂肪瘤：首例发表病例报告
Methodist Debakey Cardiovasc J. 2024 Dec 26;20(1):113-118. doi: 10.14797/mdcvj.1519. eCollection 2024.
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Congenital internal jugular vein aneurysm in an infant: A rare entity.婴儿先天性颈内静脉动脉瘤：一种罕见病症。
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[Surgical treatment of congenital spindle-shaped aneurysms of the internal jugular vein].
Vestn Khir Im I I Grek. 1975 Jan;114(1):58-63.
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Angiographic diagnosis of jugular venous system dilatation in children. A report of five cases.儿童颈静脉系统扩张的血管造影诊断。附5例报告。
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Jugular vein aneurysm.颈静脉瘤
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本文引用的文献

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A Rare Case of Internal Jugular Venous Malformation Treated by Surgical Excision.一例罕见的颈内静脉畸形通过手术切除治疗。
Methodist Debakey Cardiovasc J. 2024 Jun 11;20(1):49-53. doi: 10.14797/mdcvj.1336. eCollection 2024.
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Solitary Fibrous Tumor of Internal Jugular Vein: An Extremely Rare Entity with Review of Literature.颈内静脉孤立性纤维瘤：一种极其罕见的疾病并文献复习
Indian J Radiol Imaging. 2021 Apr;31(2):484-487. doi: 10.1055/s-0041-1734352. Epub 2021 Jul 27.
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下腔静脉和左肾静脉血管内脂肪瘤
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INTRAVASCULAR LIPOMA OF THE RIGHT BRACHIOCEPHALIC VEIN AND SUPERIOR VENA CAVA: A CASE REPORT AND LITERATURE REVIEW.右头臂静脉和上腔静脉血管内脂肪瘤：病例报告及文献复习。
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